Tag | Content |
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EnhancerAtlas ID | HS116-24299 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:113840430-113842310 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr3:113840982-113840992 | ATGGGGTGAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I114121 | chr3 | 113840198 | 113842334 |
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Enhancer Sequence | AAACTTCCAT TATTTATAAA TTTCCCAGTC TGTAGTATTT TGTTACAGCA GCAAGAATAG 60 ACTAAGACAG CTTTTAATAT GTGATTTTTA TCTAATCTTC AAATATACTA GTAAGGAAGA 120 TCGGGCTGTG GCTGGGCGCG GTGGCTCAGG CCTGTAATCC CACCACTTTG GGAGGATGAG 180 GTGGGTGGAT CACCTGAGGA CAGGAGTTCA AGATCAGTCT GACCAACAAG GTGAAACCCC 240 ATCTCTACTA AAAATACAAA AAAAAAAAAA GGAAGATCGG GCCTTCAGGT CACTGTTTTA 300 CTCACGAGGA AACTGAAGCT CATGGAGGTT AAACCACTTG CCCAAAGTAA CTTGTCTGTG 360 CTAGCACTAG AATGCCAGTC TTTGACTCAT TTCTGTTCAT TTTCTTTCCC ACAGGGTGGT 420 CAGAACCACC CTGGGTTCAG CCCAGCTCCC TCTCTGGGAC ACATGTATCC TTGGAGGCCT 480 GTAGCCACCA CTCACTCCTC TCAGTGCCCT GCAGACTATA CACAAAGCAG GAGTCAATGC 540 ACAATAATGG AGATGGGGTG ATTAATTGAG GTGAGGGTGG GTGGAACAAG AGGTCCCAGG 600 TCTTGTGCTT GGCACGAACT CTCTGGTTCT GCCTCTGCCA ATGTGTGCTG CAGACAGCTA 660 AGCTGACACT GGCATCACCT GCACTGAGTC TCTGTGTCAT GAGGTAGTCA TGGAAACTCA 720 CTCCTTCCTA AGGTAATGAG GAGACAATTA GGTAGAAATG AGAAATCGAG TTAATTGCTT 780 GTCATCCCCT CTCTGCTCTC TGTGTATTTA TTCAAATTAA GCTTTTTCAG TTTTCTAGTG 840 TCAGCAGATA CCAATGATCG GAGCACAGGC TTGGGAGCCA GGACCTCCAG GAAACAGCCA 900 GTACTGCATG AATCACTTGC CCTTCCTGCC TCTTTGTTTA GTCCTGACCC AAGCATTCAG 960 GAAAACAAAT CTCTTTGCCT GACCTCCCTT GGCTTCTGAC CGAAAGTCTC TGAACTGACT 1020 TAATTTTAAC CATCTCTGGC TCCACATGCA TTCAGCTAGT CATTCCTCTT CCTTTAGAGA 1080 AAAAGGGAGG AATTCAAATT AAATTCTACA TTTGTGGAAA TCCAGTGTAA CTCAGAGAGA 1140 TGTAGTTAAA TAAATCAGTG ATGGACGTTT TGTGGTGTGT ATTGTCCGCA TGGATGGTAA 1200 GGAGGCAAGA CCTAGAGGTC ATTTGTGAGT AGGGCCCCCA TAGGCTCAGC TGCCACTTGA 1260 GCAGAGCAGG AAAAGATCTG CCAAGATCAC ACCCTTTCCT TCCCTGTCCT TTCCGTAGGG 1320 TCTCTTCTCT ACAGCAAGAT GGAATTATTT GAAATTCCTT TCATGGTCCT TGCTTCTACT 1380 TATCTTTAGC TCTTCAGAGG TCTGCTCTGT CTAGAATGCC TTTCCTACTT TTTTATTACA 1440 TCTCAACCCT GGCAATACTT GTCCAAGAAG CCTTCTCAAG GCTGAATATG GGGCTTCCAA 1500 GTTCATGAAT TTCAAGAATT CGTGGGTTTC CAAACACCAT GAATTCTCTT TTTTATAGAC 1560 AACAAGGAGT TCATCACTGT ACGCCTAAAT TCTACTGTGG GCTAGAAGCT TCTGGGGGCA 1620 GGAACCATGT CTTCTTTTTT TTTTGAGATG GAATTTCACT GTTGTTGCCC AGGCTGGAGT 1680 ACAATGGTGC GACCATGGCT CACTGCAACC TCCACCTCGC AGGCTCAAGC GATTCTCCTC 1740 TGTCAGCCTC CCGAGTAGCT GGGATTACAG GTGCTTGCCA CCACGCTCGG CTAATTTTTG 1800 TAATTTTAGT ATAGACAAGG TTTCACCATG TTGGCTAGGC TGGTCTCGAA CACCTGGCCT 1860 CAGGTGATCC ACCCTCCTCG 1880
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